Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3-Methylcyclohexanol | HCID 11566 | — |
| Reactant | Thiophosphoryl chloride | HCID 19883 | — |
| Solvent | Trichloroethylene | HCID 6575 | — |
| Product | HCID 53681827 | HCID 53681827 | 74.8% |
Reaction Steps
A mixture of 3-methylcyclohexanol (5.0 g, 43.8 mmol) in trichloroethylene (300 mL) is added dropwise to a 0°-4° C. mixture of thiophosphoryl chloride (11.13 g, 65.7 mmol) and anhydrous pyridine (5.20 g, 65.7 mmol) in trichloroethylene (125 mL) over a 1 hour period under a nitrogen atmosphere. The resultant reaction mixture is stirred at 0°-4° C. for 1 hour and is then warmed to room temperature and stirred at room temperature for 8 hours. A white solid gradually precipitates. The white solid is filtered from the reaction mixture. The resultant reaction mixture is concentrated in vacuo to a residue. Successive aliquots of toluene (100 mL) are added to the residue and then separately are evaporated in vacuo to give 7.57 g (70%) of (3-methylcyclohexyl)-thiophosphoryl dichloride which can be used directly without further purification as the starting material for Example 23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05804569 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-56d43a3b272a4c4cad885821ea0cf8c7 |
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| Source note | uspto-grants-1998_09 |
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